Research Assistant

CenExel•Decatur, GA

12d•Onsite

About The Position

With moderate oversight, the Research Assistant I provides direct support to Clinical Research Coordinators in completing protocol-specific study goals while adhering to ICH, GCP, protocol, and site guidelines and policies. The role supports clinical trial visits, participant records, study supplies, data entry, assessments, and study monitoring activities. This is an on-site position in an indoor office environment. The role involves sitting, typing, standing, and walking, with occasional lifting of up to 20 pounds and/or pushing carts up to 50 pounds. Reporting to work as scheduled is essential. CenExel describes its work environment as promoting teamwork, positive leadership, and work-life balance. Full-time employees are eligible for a benefits package after 30 days of employment.

Requirements

High school graduate or equivalent.
Excellent computer skills and advanced knowledge of electronic equipment, including email, computers, fax machines, and copiers.
Skilled in organization and record maintenance.
Skilled in developing and maintaining effective working relationships with supervisors and coworkers.
Strong personal initiative and attention to detail.
Ability to react calmly and effectively in emergency situations.
Ability to interpret, adapt, and apply guidelines and procedures.
Ability to communicate clearly both orally and verbally.

Responsibilities

Create and maintain patient charts for assigned studies.
Prepare participant visits according to the Clinical Research Coordinator’s schedule, ensuring source documents, assessments, lab kits, and other visit materials are available and accurate.
File lab results, EKG results, and other communications in designated patient charts.
Maintain inventory of study-specific supplies, including lab kits, assessments, and participant-facing materials.
Complete data entry and resolve queries for all CRFs within sponsor-specific timelines and deadlines established in contracts or other communications.
Conduct assessments, including blood pressure measurement and urine collection.
Communicate with study participants, caregivers, third-party vendors, and laboratories as needed.
Assist Coordinators with scheduling, copying, faxing, and other clerical tasks.
Assist Coordinators in facilitating study monitoring visits.
Complete daily responsibilities delegated by the CRC as they pertain to the study and/or participants.
Assume other duties and responsibilities as assigned.